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dc.contributor.author
Castillo Scheuermann, Maria Victoria Elizabeth  
dc.contributor.author
Iramain, Maximiliano Alberto  
dc.contributor.author
Davies, Lilian Emilia  
dc.contributor.author
Manzur, Maria Eugenia  
dc.contributor.author
Brandan, Silvia Antonia  
dc.date.available
2019-10-23T13:25:43Z  
dc.date.issued
2018-02  
dc.identifier.citation
Castillo Scheuermann, Maria Victoria Elizabeth; Iramain, Maximiliano Alberto; Davies, Lilian Emilia; Manzur, Maria Eugenia; Brandan, Silvia Antonia; Evaluation of the structural properties of powerful pesticide dieldrin in different media and their complete vibrational assignment; Elsevier Science; Journal of Molecular Structure; 1154; 2-2018; 392-405  
dc.identifier.issn
0022-2860  
dc.identifier.uri
http://hdl.handle.net/11336/87060  
dc.description.abstract
Dieldrin was characterized by using Fourier Transform infrared (FT-IR) and Raman (FT-Raman), UltravioleteVisible(UVeVisible) spectroscopies. The structural and vibrational properties for dieldrin in gasphase and in aqueous solution were computed combining those experimental spectra with hybridsB3LYP and WB97XD calculations by using the 6-31G* and 6-311þþG** basis sets. Here, the experimentalavailable Hydrogen and Carbon Nuclear Magnetic Resonance (1H and 13C NMR) for dieldrin were alsoused and compared with those predicted by calculations. The B3LYP/6-311þþG** method generates themost stable structures while the results have demonstrated certain dependence of the volume and dipolemoment values with the method, size of the basis set and, with the studied media. The lower solvationenergy for dieldrin (32.94 kJ/mol) is observed for the higher contraction volume (2.4 Å3) by using theB3LYP/6-31G* method. The NBO studies suggest a high stability of dieldrin in gas phase by using theWB97XD/6-31G* method due to the n/p* and n*/p* interactions while the AIM analyses support thishigh stability by the C18/H26 and C14/O7 contacts. The different topological properties observed inthe R5 ring suggest that probably this ring plays a very important role in the toxics properties of dieldrin.The frontier orbitals show that when dieldrin is compared with other toxics substances the reactivityincreases in the following order: CO < STX < dieldrin < C6Cl6 <TCAB < TCAOB < CN where evidently, thepresence of five rings and six Cl atoms decrease the reactivity of dieldrin, as compared with hexachlorobencene.The WB97XD method and the two basis sets predicted for dieldrin in both media lowreactivities, higher nucleophilicity and, low electrophilicity. All the bands observed in the IR and Ramanspectra were completely assigned to the 75 vibration normal modes and their harmonic force fields andforce constants for first time are reported for dieldrin. The predicted FTIR, FT-Raman, UVeVisible and 1Hand 13C NMR spectra for dieldrin show a reasonable concordance with the experimental ones.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
DIELDRIN  
dc.subject
VIBRATIONAL SPECTRA  
dc.subject
DFT  
dc.subject.classification
Otras Ciencias Químicas  
dc.subject.classification
Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Evaluation of the structural properties of powerful pesticide dieldrin in different media and their complete vibrational assignment  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-10-22T17:25:21Z  
dc.journal.volume
1154  
dc.journal.pagination
392-405  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Holanda  
dc.description.fil
Fil: Castillo Scheuermann, Maria Victoria Elizabeth. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia; Argentina  
dc.description.fil
Fil: Iramain, Maximiliano Alberto. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina  
dc.description.fil
Fil: Davies, Lilian Emilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina  
dc.description.fil
Fil: Manzur, Maria Eugenia. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia; Argentina  
dc.description.fil
Fil: Brandan, Silvia Antonia. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia; Argentina  
dc.journal.title
Journal of Molecular Structure  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0022286017314126?via%3Dihub  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://doi.org/10.1016/j.molstruc.2017.10.065